01 2ARAGEN LIFE SCIENCES LIMITED Hyderabad IN
02 1BIOINDUSTRIA L.I.M. S.P.A. Novi Ligure IT
03 1EXCELLA GMBH & CO. KG Feucht DE
04 1HAINAN POLY PHARMACEUTICAL COMPANY LIMITED Haikou CN
05 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. Milano IT
06 1SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
01 6Dobutamine hydrochloride
02 1Dobutamine hydrochloride, Process-2
01 1China
02 1Germany
03 2India
04 2Italy
05 1Switzerland
01 6Valid
02 1Withdrawn by Holder
Dobutamine Hydrochloride, Process-2
Certificate Number : CEP 2020-180 - Rev 03
Status : Valid
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 1200
Certificate Number : R0-CEP 2016-106 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2021-02-22
Type : Chemical
Substance Number : 1200
Certificate Number : R1-CEP 2004-261 - Rev 01
Status : Valid
Issue Date : 2018-03-07
Type : Chemical
Substance Number : 1200
Certificate Number : R0-CEP 2020-415 - Rev 00
Status : Valid
Issue Date : 2021-09-22
Type : Chemical
Substance Number : 1200
Certificate Number : CEP 2017-291 - Rev 01
Status : Valid
Issue Date : 2024-03-01
Type : Chemical
Substance Number : 1200
Certificate Number : R1-CEP 2006-273 - Rev 01
Status : Valid
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 1200
Certificate Number : R1-CEP 2002-173 - Rev 03
Status : Valid
Issue Date : 2016-12-09
Type : Chemical
Substance Number : 1200
A Dobutamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dobutamine Hydrochloride, including repackagers and relabelers. The FDA regulates Dobutamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dobutamine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Dobutamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dobutamine Hydrochloride supplier is an individual or a company that provides Dobutamine Hydrochloride active pharmaceutical ingredient (API) or Dobutamine Hydrochloride finished formulations upon request. The Dobutamine Hydrochloride suppliers may include Dobutamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dobutamine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dobutamine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Dobutamine Hydrochloride Certificate of Suitability (COS). The purpose of a Dobutamine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dobutamine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dobutamine Hydrochloride to their clients by showing that a Dobutamine Hydrochloride CEP has been issued for it. The manufacturer submits a Dobutamine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dobutamine Hydrochloride CEP holder for the record. Additionally, the data presented in the Dobutamine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dobutamine Hydrochloride DMF.
A Dobutamine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dobutamine Hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Dobutamine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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